CN1062908C - 新多肽和编码它们的脱氧核糖核酸 - Google Patents
新多肽和编码它们的脱氧核糖核酸 Download PDFInfo
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- CN1062908C CN1062908C CN94117067A CN94117067A CN1062908C CN 1062908 C CN1062908 C CN 1062908C CN 94117067 A CN94117067 A CN 94117067A CN 94117067 A CN94117067 A CN 94117067A CN 1062908 C CN1062908 C CN 1062908C
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- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/24—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
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JP28050593 | 1993-10-14 | ||
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CN1110323A CN1110323A (zh) | 1995-10-18 |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2751658B1 (fr) * | 1996-07-26 | 1998-10-02 | Pasteur Institut | Utilisation d'une chemokine (sdf-1) ligand pour le recepteur de lestr/fusin/cxcr4 pour prevenir ou traiter l'infection par des virus de type vih |
AU737910B2 (en) * | 1997-01-31 | 2001-09-06 | Regents Of The University Of California, The | Chimeric antibody fusion proteins for the recruitment and stimulation of an antitumor immune response |
US6100387A (en) * | 1997-02-28 | 2000-08-08 | Genetics Institute, Inc. | Chimeric polypeptides containing chemokine domains |
US6852508B1 (en) * | 1997-02-28 | 2005-02-08 | Genetics Institute, Llc | Chemokine with amino-terminal modifications |
DE19734161A1 (de) * | 1997-08-07 | 1999-04-01 | Jerini Biotools Gmbh | SDF-1 - Antagonisten |
MXPA00003885A (es) * | 1997-10-22 | 2004-04-23 | Inst Genetics Llc | Quimiocinas con modificiaciones de la terminacion amino. |
AU762472B2 (en) * | 1998-03-13 | 2003-06-26 | University Of British Columbia, The | Therapeutic chemokine receptor antagonists |
CA2245224A1 (en) * | 1998-08-14 | 2000-02-14 | Jiang-Hong Giong | Chemokine receptor antagonists and chemotherapeutics |
CA2305787A1 (en) * | 2000-05-09 | 2001-11-09 | The University Of British Columbia | Cxcr4 antagonist treatment of hematopoietic cells |
ATE333896T1 (de) * | 1998-03-24 | 2006-08-15 | Chugai Pharmaceutical Co Ltd | Vaskularisierungsinhibitoren |
CA2731416A1 (en) * | 1998-03-30 | 1999-10-07 | Northwest Biotherapeutics, Inc. | Therapeutic and diagnostic applications based on the role of the cxcr-4 gene in tumorigenesis |
US7157418B1 (en) | 1998-07-22 | 2007-01-02 | Osprey Pharmaceuticals, Ltd. | Methods and compositions for treating secondary tissue damage and other inflammatory conditions and disorders |
US20030215421A1 (en) * | 1999-07-21 | 2003-11-20 | Mcdonald John R. | Methods and compositions for treating secondary tissue damage and other inflammatory conditions and disorders |
AU5241099A (en) * | 1998-07-31 | 2000-02-21 | Trustees Of Columbia University In The City Of New York, The | Use of inhibitors of the activation of cxcr4 receptor by sdf-1 in treating rheumatoid arthritis |
US6448054B1 (en) | 1999-04-08 | 2002-09-10 | The General Hospital Corporation | Purposeful movement of human migratory cells away from an agent source |
US6949243B1 (en) * | 1999-11-24 | 2005-09-27 | Schering Corporation | Methods of inhibiting metastasis |
US20050059584A1 (en) * | 2002-08-16 | 2005-03-17 | Ahmed Merzouk | Novel chemokine mimetics synthesis and their use |
CA2335109A1 (en) * | 2000-04-12 | 2001-10-12 | Chemokine Therapeutics Corporation | Cxcr4 agonist treatment of hematopoietic cells |
US7368425B2 (en) * | 2006-03-24 | 2008-05-06 | Chemokine Therapeutics Corp. | Cyclic peptides for modulating growth of neo-vessels and their use in therapeutic angiogenesis |
US7378098B2 (en) * | 2000-04-12 | 2008-05-27 | The University Of British Columbia | CXC chemokine receptor 4 agonist peptides |
DE10027383A1 (de) * | 2000-06-02 | 2001-12-20 | Rhein Biotech Proz & Prod Gmbh | Nukleinsäure-Molekül umfassend eine für ein Chemokin, einen Neuropeptid-Präkursor oder mindestens ein Neuropeptid kodierende Nukleinsäuresequenz |
US20020094327A1 (en) * | 2000-11-05 | 2002-07-18 | Petersen Bryon E. | Targeting pluripotent stem cells to tissues |
JP2004155010A (ja) | 2002-11-06 | 2004-06-03 | Sony Corp | 可逆性多色記録媒体、及びこれを用いた記録方法 |
JP2004074583A (ja) | 2002-08-19 | 2004-03-11 | Sony Corp | 可逆性多色記録媒体、及びこれを用いた記録方法 |
WO2006032144A1 (en) * | 2004-09-23 | 2006-03-30 | Arc Pharmaceuticals, Inc. | Pharmaceutical compositions and methods relating to inhibiting fibrous adhesions or inflammatory disease using fucans from various echinoderm sources |
CA2581237C (en) * | 2004-09-24 | 2018-11-06 | Angioblast Systems, Inc. | Method of enhancing proliferation and/or survival of mesenchymal precursor cells (mpc) |
WO2006137934A2 (en) | 2004-11-05 | 2006-12-28 | The General Hospital Corporation | Purposeful movement of human migratory cells away from an agent source |
US20060264365A1 (en) * | 2005-05-18 | 2006-11-23 | Hung Li | Treatment of brain tissue damage |
WO2007048846A1 (de) * | 2005-10-27 | 2007-05-03 | Neuraxo Biopharmaceuticals Gmbh | Verwendung von eisen chelatisierenden verbindungen, zyklisches adenosinmonophosphat erhöhende verbindungen oder kombinationen davon zur behandlung von axonalen läsionen im zns |
EP1942940A2 (en) * | 2005-10-31 | 2008-07-16 | Laboratoires Serono SA | Use of sdf-1 for the treatment and/or prevention of neurological diseases |
CN100432106C (zh) * | 2006-06-02 | 2008-11-12 | 广东省微生物研究所 | 一种附着法保藏抗菌肽的方法 |
EP2049146A2 (en) * | 2006-07-07 | 2009-04-22 | Hans-Werner Müller | Use of proteins of the sdf-1-family for for improvement of axonal plasticity or for axonal regeneration following lesions |
CN103897058B (zh) | 2006-10-02 | 2018-06-15 | E.R.施贵宝&圣斯有限责任公司 | 结合cxcr4的人类抗体及其用途 |
US7696309B2 (en) | 2006-10-23 | 2010-04-13 | The Brigham And Women's Hospital, Inc. | Protease resistant mutants of stromal cell derived factor-1 in the repair of tissue damage |
WO2008096359A2 (en) * | 2007-02-08 | 2008-08-14 | Rappaport Family Institute For Research In The Medical Sciences | Agents for the treatment of multiple sclerosis and methods of using same |
KR100767841B1 (ko) | 2007-03-30 | 2007-10-18 | 주식회사 욱성 | 3중층 구조의 경편직물로 구성한 타이어체인 |
US8263064B2 (en) | 2007-06-04 | 2012-09-11 | Rappaport Family Institute For Research In The Medical Sciences | Method of suppressing disease severity of multiple sclerosis using chemokine CXC11 |
WO2009073911A1 (en) | 2007-12-10 | 2009-06-18 | Mater Medical Research Institute | Treatment and prophylaxis |
CN101229184B (zh) * | 2008-01-17 | 2010-08-11 | 周锡漳 | 一种脱氧核糖核酸降解片段复合物及其制备药物的应用 |
WO2011106234A1 (en) | 2010-02-25 | 2011-09-01 | Provasculon, Inc. | Protease-resistant mutants of stromal cell derived factor-1 in the repair of tissue damage |
WO2012037083A2 (en) * | 2010-09-15 | 2012-03-22 | The Cleveland Clinic Foundation | Compositions and method for promoting musculoskeletal repair |
JP6145089B2 (ja) | 2011-06-07 | 2017-06-07 | メソブラスト インターナショナル エスエイアールエル | ストロマ細胞由来因子−1のプロテアーゼ耐性変異体を用いた、組織損傷を修復するための方法 |
SG11201401386XA (en) | 2011-11-09 | 2014-10-30 | Bristol Myers Squibb Co | Treatment of hematologic malignancies with an anti-cxcr4 antibody |
US9908923B2 (en) | 2014-06-11 | 2018-03-06 | The Medical College Of Wisconsin, Inc. | Monomeric CXCL121 peptide and methods of use thereof |
DK3050574T3 (da) | 2015-01-28 | 2020-01-20 | Univ Bordeaux | Anvendelse af plerixafor til behandling og/eller forebyggelse af akutte forværringer af kronisk obstruktiv lungesygdom |
WO2016191811A1 (en) | 2015-06-03 | 2016-12-08 | The University Of Queensland | Mobilizing agents and uses therefor |
WO2019070538A1 (en) | 2017-10-03 | 2019-04-11 | Wallkill BioPharma, Inc. | TREATMENT OF DIABETES WITH GENETICALLY MODIFIED BETA CELLS |
KR102381876B1 (ko) * | 2021-10-27 | 2022-04-01 | 홍천석 | 전선터미널 압착시스템 |
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JP2879303B2 (ja) * | 1993-01-14 | 1999-04-05 | 佑 本庶 | cDNAライブラリーの作製方法、および新規なポリペプチドとそれをコードするDNA |
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- 1994-10-13 PT PT94116169T patent/PT657468E/pt unknown
- 1994-10-13 ES ES94116169T patent/ES2244955T3/es not_active Expired - Lifetime
- 1994-10-13 DK DK94116169T patent/DK0657468T3/da active
- 1994-10-13 AT AT94116169T patent/ATE299891T1/de active
- 1994-10-13 EP EP94116169A patent/EP0657468B1/en not_active Expired - Lifetime
- 1994-10-13 DE DE69434428T patent/DE69434428T2/de not_active Expired - Lifetime
- 1994-10-14 US US08/323,084 patent/US5563048A/en not_active Expired - Lifetime
- 1994-10-14 CN CN94117067A patent/CN1062908C/zh not_active Expired - Lifetime
- 1994-11-24 TW TW083111031A patent/TW302369B/zh not_active IP Right Cessation
-
1996
- 1996-07-01 US US08/674,008 patent/US5756084A/en not_active Expired - Lifetime
-
2000
- 2000-06-08 JP JP2000171523A patent/JP3705732B2/ja not_active Expired - Lifetime
-
2005
- 2005-06-16 JP JP2005176246A patent/JP2005336198A/ja not_active Withdrawn
-
2007
- 2007-07-06 JP JP2007178072A patent/JP2007291132A/ja not_active Withdrawn
Non-Patent Citations (1)
Title |
---|
BIOCHENISTRY VOL 29 1990.1.1;PROC NATL ACAD SCI VOL 77 NO12 1980.1.1 * |
Also Published As
Publication number | Publication date |
---|---|
ATE299891T1 (de) | 2005-08-15 |
PT657468E (pt) | 2005-10-31 |
US5756084A (en) | 1998-05-26 |
CA2117953C (en) | 2001-12-11 |
CA2117953A1 (en) | 1995-04-15 |
EP1557428A1 (en) | 2005-07-27 |
DE69434428T2 (de) | 2006-05-24 |
JP3705732B2 (ja) | 2005-10-12 |
KR100210308B1 (ko) | 1999-07-15 |
JP2005336198A (ja) | 2005-12-08 |
US5563048A (en) | 1996-10-08 |
DE69434428D1 (de) | 2005-08-25 |
TW302369B (enrdf_load_stackoverflow) | 1997-04-11 |
KR950011618A (ko) | 1995-05-15 |
EP0657468A1 (en) | 1995-06-14 |
JP2001017191A (ja) | 2001-01-23 |
JP3367581B2 (ja) | 2003-01-14 |
EP0657468B1 (en) | 2005-07-20 |
JPH07188294A (ja) | 1995-07-25 |
CN1110323A (zh) | 1995-10-18 |
ES2244955T3 (es) | 2005-12-16 |
JP2007291132A (ja) | 2007-11-08 |
DK0657468T3 (da) | 2005-08-08 |
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